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Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events

Cite this dataset

Shahbaba, Babak et al. (2021). Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events [Dataset]. Dryad. https://doi.org/10.7280/D14X30

Abstract

The hippocampus is critical to the temporal organization of our experiences. Although this fundamental capacity is conserved across modalities and species, its underlying neuronal mechanisms remain unclear. Here we recorded hippocampal activity as rats remembered an extended sequence of nonspatial events and, using novel statistical methods, uncovered new forms of sequential organization in ensemble activity important for order memory judgments. Specifically, we discovered that hippocampal ensembles provide significant temporal coding throughout nonspatial event sequences, differentiate distinct types of task-critical information sequentially within events, exhibit theta-associated replay of the sequential relationships among events, and can represent past, present and future events within individual theta cycles. These findings suggest a fundamental function of the hippocampal network is to encode, preserve, and predict the sequential order of experiences.

README: Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events

<https://doi.org/10.7280/D14X30>

Shahbaba et al., 2021 Data repository

Readme drafted on October XX, 2021

Contents

Project summary
Contact information
Dataset Citation
References using this data
Data collection methods and behavior
Description of files
Associated code
Directory Manifest

1. Project summary

The hippocampus is critical to the temporal organization of our experiences. Although this fundamental capacity is conserved across modalities and species, its underlying neuronal mechanisms remain unclear. Our work and others suggest a fundamental function of the hippocampal network is to encode, preserve, and predict the sequential order of experiences.

Here, this dataset contains tetrode extracellular recordings from hippocampus (local field potentials and sorted unit spikes) from five male Long–Evans rats. These recordings were performed using a custom electrode microdrive array, positioned along the dorsal axis of the hippocampus, while the rats performed a complex odor sequence memory task.

2. Contact information

Norbert Fortin (Principal investigator)
<norbert.fortin@uci.edu>

Keiland Cooper (For questions regarding the dataset or documentation)
<kwcooper@uci.edu>

3. Dataset Citation

TBD

4. References using this data

Allen, T. A., Salz, D. M., McKenzie, S. & Fortin, N. J. Nonspatial sequence coding in CA1 neurons. J. Neurosci. 36, 1547–1563 (2016).

Shahbaba, B., Li, L., Agostinelli, F., Saraf, M., Cooper, K. W., Haghverdian, D., Elias, G. A., Baldi, P., & Fortin, N. J. (2021). Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events. Nature Communications. (In press)

5. Data collection methods and behavior

For more information on data collection and procedures, please see the included references.

Recording device and surgery
Each chronically implanted custom microdrive contained 20 independently drivable tetrodes. Each tetrode consisted of four twisted nichrome wire (13 µm in diameter; California Fine Wire) and gold-plated to achieve final tip impedance of ~250 kΩ (measured at 1 kHz). Voltage signals recorded from the tetrode tips were referenced to a ground screw positioned over the cerebellum, and filtered for single-unit activity (154 Hz to 8.8 kHz). The neural signals were then amplified (10,000–32,000X), digitized (40 kHz) and recorded to disk with the data acquisition system (MAP, Plexon). The microdrive was implanted over the left hippocampus, centered on coordinates: -4.0 mm AP, 3.5 mm ML.

Unit preprocessing and spike sorting
Action potentials from individual neurons were manually isolated offline using a combination of standard waveform features across the four channels of each tetrode (Offline Sorter, Plexon). Proper isolation was verified using interspike interval distributions for each isolated unit (assuming a minimum refractory period of 1 ms) and cross-correlograms for each pair of simultaneously recorded units on the same tetrode.

Odor sequence task
Naïve rats were initially trained to nosepoke and reliably hold their nose for 1.2 s in the odor port for a water reward. Odor sequences of increasing length were then introduced in successive stages (A, AB, ABC, ABCD, and ABCDE) upon reaching behavioral criterion of 80% correct over three sessions per training stage. In each stage, rats were trained to correctly identify each presented item as either InSeq (by holding their nosepoke response for at least 1.2 s to receive a water reward) or OutSeq (by withdrawing their nose before 1.2 s to receive a reward). Note that OutSeq items could be presented in any sequence position except the first (i.e., sequences always began with odor A, though odor A could also be presented later in the sequence as an OutSeq item).

All procedures were conducted in accordance with the Institutional Animal Care and Use Committee (Boston University and University of California, Irvine).

6. Description of files

Please see the included README file (within Shahbaba_2021_dataset folder).

Methods

Recording device and surgery

Each chronically implanted custom microdrive contained 20 independently drivable tetrodes. Each tetrode consisted of four twisted nichrome wire (13 µm in diameter; California Fine Wire) and gold-plated to achieve final tip impedance of ~250 kΩ (measured at 1 kHz). Voltage signals recorded from the tetrode tips were referenced to a ground screw positioned over the cerebellum, and filtered for single-unit activity (154 Hz to 8.8 kHz). The neural signals were then amplified (10,000–32,000X), digitized (40 kHz) and recorded to disk with the data acquisition system (MAP, Plexon). The microdrive was implanted over the left hippocampus, centered on coordinates: -4.0 mm AP, 3.5 mm ML. 

Unit preprocessing and spike sorting

Action potentials from individual neurons were manually isolated offline using a combination of standard waveform features across the four channels of each tetrode (Offline Sorter, Plexon). Proper isolation was verified using interspike interval distributions for each isolated unit (assuming a minimum refractory period of 1 ms) and cross-correlograms for each pair of simultaneously recorded units on the same tetrode.

Odor sequence task

Five naïve rats were initially trained to nosepoke and reliably hold their nose for 1.2 s in the odor port for a water reward. Odor sequences of increasing length were then introduced in successive stages (A, AB, ABC, ABCD, and ABCDE) upon reaching behavioral criterion of 80% correct over three sessions per training stage. In each stage, rats were trained to correctly identify each presented item as either InSeq (by holding their nosepoke response for at least 1.2 s to receive a water reward) or OutSeq (by withdrawing their nose before 1.2 s to receive a reward). Note that OutSeq items could be presented in any sequence position except the first (i.e., sequences always began with odor A, though odor A could also be presented later in the sequence as an OutSeq item).

All procedures were conducted in accordance with the Institutional Animal Care and Use Committee (Boston University and University of California, Irvine).

For more information on data collection and procedures, please see the included references or feel free to contact us! 

Usage notes

Please see the included README file.

Funding

National Institute of Mental Health, Award: R01-MH115697

National Institute on Deafness and Other Communication Disorders, Award: R01-DC017687

National Cancer Institute, Award: T32-DC010775

National Science Foundation, Award: DGE-1839285

National Science Foundation, Award: IOS-1150292

National Science Foundation, Award: BCS-1439267

Whitehall Foundation, Award: 2010-05-84